JPS6143355B2 - - Google Patents
Info
- Publication number
- JPS6143355B2 JPS6143355B2 JP58136917A JP13691783A JPS6143355B2 JP S6143355 B2 JPS6143355 B2 JP S6143355B2 JP 58136917 A JP58136917 A JP 58136917A JP 13691783 A JP13691783 A JP 13691783A JP S6143355 B2 JPS6143355 B2 JP S6143355B2
- Authority
- JP
- Japan
- Prior art keywords
- ticlopidine
- platelet aggregation
- activity
- hcl
- tetrahydrothieno
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- IULJSGIJJZZUMF-UHFFFAOYSA-N 2-hydroxybenzenesulfonic acid Chemical class OC1=CC=CC=C1S(O)(=O)=O IULJSGIJJZZUMF-UHFFFAOYSA-N 0.000 claims abstract description 7
- 150000003839 salts Chemical class 0.000 claims description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 4
- 101000783577 Dendroaspis angusticeps Thrombostatin Proteins 0.000 claims description 3
- 101000783578 Dendroaspis jamesoni kaimosae Dendroaspin Proteins 0.000 claims description 3
- 229940127218 antiplatelet drug Drugs 0.000 claims description 3
- 239000000106 platelet aggregation inhibitor Substances 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 2
- MVIOINXPSFUJEN-UHFFFAOYSA-N benzenesulfonic acid;hydrate Chemical compound O.OS(=O)(=O)C1=CC=CC=C1 MVIOINXPSFUJEN-UHFFFAOYSA-N 0.000 claims 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims 2
- VSAZFRKEFQPOIS-UHFFFAOYSA-N 2,5-dihydroxybenzene-1,4-disulfonic acid Chemical compound OC1=CC(S(O)(=O)=O)=C(O)C=C1S(O)(=O)=O VSAZFRKEFQPOIS-UHFFFAOYSA-N 0.000 claims 1
- IKQCSJBQLWJEPU-UHFFFAOYSA-N 2,5-dihydroxybenzenesulfonic acid Chemical compound OC1=CC=C(O)C(S(O)(=O)=O)=C1 IKQCSJBQLWJEPU-UHFFFAOYSA-N 0.000 claims 1
- PHWBOXQYWZNQIN-UHFFFAOYSA-N ticlopidine Chemical class ClC1=CC=CC=C1CN1CC(C=CS2)=C2CC1 PHWBOXQYWZNQIN-UHFFFAOYSA-N 0.000 abstract description 20
- 208000010110 spontaneous platelet aggregation Diseases 0.000 abstract description 11
- 230000000694 effects Effects 0.000 abstract description 8
- 230000002401 inhibitory effect Effects 0.000 abstract description 5
- 210000004369 blood Anatomy 0.000 abstract description 4
- 239000008280 blood Substances 0.000 abstract description 4
- 150000002632 lipids Chemical class 0.000 abstract description 2
- 230000002168 angioprotective effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 229960005001 ticlopidine Drugs 0.000 description 14
- 229940079593 drug Drugs 0.000 description 13
- 239000003814 drug Substances 0.000 description 13
- 239000005528 B01AC05 - Ticlopidine Substances 0.000 description 7
- 241001465754 Metazoa Species 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 210000004623 platelet-rich plasma Anatomy 0.000 description 4
- 241000700159 Rattus Species 0.000 description 3
- 241000700157 Rattus norvegicus Species 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 230000035699 permeability Effects 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000002666 vasoprotective effect Effects 0.000 description 2
- VZYDKJOUEPFKMW-UHFFFAOYSA-N 2,3-dihydroxybenzenesulfonic acid Chemical compound OC1=CC=CC(S(O)(=O)=O)=C1O VZYDKJOUEPFKMW-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- IVOMOUWHDPKRLL-KQYNXXCUSA-N Cyclic adenosine monophosphate Chemical compound C([C@H]1O2)OP(O)(=O)O[C@H]1[C@@H](O)[C@@H]2N1C(N=CN=C2N)=C2N=C1 IVOMOUWHDPKRLL-KQYNXXCUSA-N 0.000 description 1
- 102000016359 Fibronectins Human genes 0.000 description 1
- 108010067306 Fibronectins Proteins 0.000 description 1
- 229920004011 Macrolon® Polymers 0.000 description 1
- 229920003091 Methocel™ Polymers 0.000 description 1
- IVOMOUWHDPKRLL-UHFFFAOYSA-N UNPD107823 Natural products O1C2COP(O)(=O)OC2C(O)C1N1C(N=CN=C2N)=C2N=C1 IVOMOUWHDPKRLL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 230000002785 anti-thrombosis Effects 0.000 description 1
- 239000003146 anticoagulant agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 229940095074 cyclic amp Drugs 0.000 description 1
- 238000001647 drug administration Methods 0.000 description 1
- KAQKFAOMNZTLHT-VVUHWYTRSA-N epoprostenol Chemical compound O1C(=CCCCC(O)=O)C[C@@H]2[C@@H](/C=C/[C@@H](O)CCCCC)[C@H](O)C[C@@H]21 KAQKFAOMNZTLHT-VVUHWYTRSA-N 0.000 description 1
- 229960001123 epoprostenol Drugs 0.000 description 1
- 210000003743 erythrocyte Anatomy 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 238000012261 overproduction Methods 0.000 description 1
- 229940094443 oxytocics prostaglandins Drugs 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 150000003180 prostaglandins Chemical class 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical class OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT22600-A/82 | 1982-07-28 | ||
| IT8222600A IT8222600A0 (it) | 1982-07-28 | 1982-07-28 | Nuovi idrossibenzensolfonati della 5-(o-clorobenzil)-4,5,6,7-tetraidro tieno parentesi quadra aperta 3,2-c parentesi quadra chiusa piridina. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5942388A JPS5942388A (ja) | 1984-03-08 |
| JPS6143355B2 true JPS6143355B2 (it) | 1986-09-26 |
Family
ID=11198302
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58136917A Granted JPS5942388A (ja) | 1982-07-28 | 1983-07-28 | ５−（０−クロロベンジル）−４，５，６，７−ラトラヒドロチエ）（３，２−ｃ）ピリジンのヒドロキシベンゼンスルホン酸塩および該ヒドロキシベンゼンスルホン酸塩を有効成分とする血 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4554278A (it) |
| EP (1) | EP0099988B1 (it) |
| JP (1) | JPS5942388A (it) |
| AT (1) | ATE20067T1 (it) |
| DE (1) | DE3363731D1 (it) |
| IT (1) | IT8222600A0 (it) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2612777A1 (fr) * | 1987-03-26 | 1988-09-30 | Inst Nat Sante Rech Med | Composition medicamenteuse pour le traitement et la prevention de maladies dues a une cytotoxicite a mediation cellulaire, renfermant au moins un derive de la pyridine comme principe actif |
| ES2015433A6 (es) * | 1989-08-03 | 1990-08-16 | Esteve Quimica Sa | Procedimientos de preparacion de la sal de piperacina del monotosilato del acido 2,5-dihidroxibencenosulfonico |
| JP4605726B2 (ja) * | 1997-09-02 | 2011-01-05 | 日本曹達株式会社 | フェノール誘導体を成分化合物とする分子化合物 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR6163M (it) * | 1966-01-20 | 1968-07-08 | ||
| JPS5231357A (en) * | 1976-07-09 | 1977-03-09 | Sanken Electric Co Ltd | Chopper type dc power device |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2215948B1 (it) * | 1973-02-01 | 1976-05-14 | Centre Etd Ind Pharma | |
| US4127580A (en) * | 1975-02-07 | 1978-11-28 | Parcor | Process for the preparation of thieno-pyridine derivatives |
| FR2395983A1 (fr) * | 1977-06-29 | 1979-01-26 | Le Hao Dong | Derives de propylamine, leur procede de preparation et leur application en therapeutique |
-
1982
- 1982-07-28 IT IT8222600A patent/IT8222600A0/it unknown
-
1983
- 1983-06-23 EP EP83106166A patent/EP0099988B1/en not_active Expired
- 1983-06-23 DE DE8383106166T patent/DE3363731D1/de not_active Expired
- 1983-06-23 AT AT83106166T patent/ATE20067T1/de not_active IP Right Cessation
- 1983-07-28 US US06/517,916 patent/US4554278A/en not_active Expired - Fee Related
- 1983-07-28 JP JP58136917A patent/JPS5942388A/ja active Granted
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR6163M (it) * | 1966-01-20 | 1968-07-08 | ||
| JPS5231357A (en) * | 1976-07-09 | 1977-03-09 | Sanken Electric Co Ltd | Chopper type dc power device |
Also Published As
| Publication number | Publication date |
|---|---|
| IT8222600A0 (it) | 1982-07-28 |
| JPS5942388A (ja) | 1984-03-08 |
| EP0099988A1 (en) | 1984-02-08 |
| ATE20067T1 (de) | 1986-06-15 |
| DE3363731D1 (de) | 1986-07-03 |
| US4554278A (en) | 1985-11-19 |
| EP0099988B1 (en) | 1986-05-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU1349700A3 (ru) | Способ получени (2-оксо-1,2,3,5-тетрагидроимидазо-/2,1- @ /хиназолинил)оксиалкиламидов,их оптических изомеров или фармакологически приемлемых солей с кислотами | |
| EP0811623A1 (de) | Xanthinverbindungen mit terminal aminierten Alkinol-Seitenketten | |
| HU182801B (en) | Process for preparing n-substituted aziridine-2-carboxylic acid derivatives | |
| IE64760B1 (en) | 4-Quinoline carboxylic acid derivatives useful as immunosuppressive agents | |
| US20100144780A1 (en) | Salts and Mixture of 9-Oxoacridine-10-Acetic Acid with 1-Alkylamino-1-Desoxy-Polyols, Pharmaceutical Compositions Containing Said Agents and Treatment Methods | |
| EP0154887B1 (en) | New 2,5-diaryl tetrahydrothiophenes and analogs thereof as paf-antagonists | |
| AU599034B2 (en) | Furosemide salts | |
| JPS6143355B2 (it) | ||
| FI91750C (fi) | Menetelmä valmistaa farmaseuttisesti käyttökelpoista bentso-3,4-dihydropyridiinin johdosta | |
| KR100979077B1 (ko) | 벤즈아제핀 화합물의 고체 염 및 이를 포함하는 약제학적 조성물 | |
| JPH013197A (ja) | 抗ウイルス化合物およびそれを含有する抗ウイルス剤 | |
| US4055561A (en) | α-Alkylbenzyl lactamimides | |
| US6197767B1 (en) | Arglabin compounds and therapeutic uses thereof | |
| CA1142530A (en) | Immunestimulating n-substituted aziridine- 2-carboxylic acid derivatives | |
| US4845102A (en) | Therapeutic agent for the treatment of peptic ulcer disease | |
| EP0301428A2 (de) | Benzyldiaminopyrimidin-Derivate und deren Verwendung als Arzneimittel | |
| AU2022233178A1 (en) | Compositions and methods for treating polycythemia | |
| US3901914A (en) | 1-(substituted phosphinothioyl, phosphinyl or phosphino)-substituted indole-3-acetic acids | |
| HU197511B (en) | Process for producing pharmaceuticals with immunsuppressant effect | |
| EP0047011B1 (en) | Pharmaceutical compositions containing 4-((6,7-dihalogen-2,3-dihydro-1-oxo-1h-inden-5-yl)-oxy) butanoic acid compounds | |
| EP0623623B1 (en) | 2-aminoethanesulfonic acid/zinc complex | |
| US3344186A (en) | 2-guanidino-1, 2, 3, 4-tetrahydronaphthalene and salts thereof | |
| DE3783758T2 (de) | Verbindungen vom taurintyp. | |
| US6693127B1 (en) | Pharmaceutical compositions of arglabin and arglabin derivatives | |
| Rakoczy et al. | Salts of α-Amino-p-toluenesulfonamide |